Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g10140 | A09 | 5595941 | C | T | stop_gained | HIGH | c.857G>A|p.Trp286* |
S6 |
2 | BAA09g10140 | A09 | 5596116 | G | A | missense_variant | MODERATE | c.682C>T|p.Arg228Trp |
S233 |
3 | BAA09g10140 | A09 | 5596248 | C | T | missense_variant | MODERATE | c.550G>A|p.Asp184Asn |
S120 |
4 | BAA09g10140 | A09 | 5598313 | G | A | upstream_gene_variant | MODIFIER | c.-1516C>T| |
S32 |
5 | BAA09g10140 | A09 | 5599944 | G | A | upstream_gene_variant | MODIFIER | c.-3147C>T| |
S176 |
6 | BAA09g10140 | A09 | 5600215 | G | A | upstream_gene_variant | MODIFIER | c.-3418C>T| |
S244 |
7 | BAA09g10140 | A09 | 5601083 | C | T | upstream_gene_variant | MODIFIER | c.-4286G>A| |
S136 |
8 | BAA09g10140 | A09 | 5601233 | C | T | upstream_gene_variant | MODIFIER | c.-4436G>A| |
S148 S210 |
9 | BAA09g10140 | A09 | 5601702 | C | T | upstream_gene_variant | MODIFIER | c.-4905G>A| |
S193 |